Abstract:
Introduction. Brain abscess is a focal area of necrosis with a surrounding membrane within the brain
parenchyma, that begins as a localised area of cerebritis and develops into a collection of pus surrounded by a
well-vascularized capsule. It results from an infectious process or, rarely from a traumatic process. It can
originate from infections in head and neck sites (such as mastoiditis or sinus infection). Various conditions can
cause hematogenous seeding of the brain and the most common ones include pulmonary infections, such as lung
abscess, pneumonia and pulmonary arteriovenous malformations. Cyanotic congenital heart diseases in children
are associated in most of the cases. Brain abscesses associated with bacteremia commonly cause multiple
abscesses, mostly in the distribution of the middle cerebral artery and usually at the grey-white matter junction.
The most frequent microbial pathogens isolated from brain abscesses are Staphylococcus aureus and Viridian
streptococci. Brain abscess in newborns is a very rare disease. It can lead to elevated intracranial pressure and
has significant morbidity and mortality.
Case presentation. We will present the case of a 33-day-old male neonate with a complaint of fever for 9 days
and multiple episodes of multifocal seizures for 6 days. He was born full term by caesarean section with a birth
weight of 2.7 kg and cried immediately after birth. There was no history of maternal fever, rashes, vaginal
discharge, or bleeding during the antenatal period. The infant was diagnosed with hypospadias and sent for
examination by a paediatric surgeon. Examination of other systems revealed tachypnea, a-normal vesicular
breath sounds in upper respiratory tract, tachyarrhythmia causing racing heart rate with systolic murmur at left
sternal border. The rest of the systemic examination was normal. Magnetic resonance imaging (MRI) was
subsequently performed and revealed a large well-encapsulated cystic formation with rupture into the left
ventricle (brain abscess) and intracranial haemorrhage. Chest CT reveals Pneumonia Totalis Sinistra. Laboratory
investigations showed a positive sepsis screen, anaemia and hypoproteinemia. After that, an emergency
operation was undertaken. The infant was intubated and an aspiration was undertaken through a left frontal burr
hole under local anaesthesia and about 300 ml of thin yellow pus was evacuated slowly. A left temporal
craniotomy was undertaken for evacuation of the hematoma. After finishing the operation the baby was admitted
to the Neonatal Intensive Care Unit. An improvement in general condition was observed, following which, the
neonate started feeding well and was subsequently discharged after 3 weeks of therapy.
Discussion. Brain abscess is a rare condition in neonates and infants. Only a few large cases have been
published. Some clinical presentations of brain abscess in the neonatal period require surgical intervention. This
case was characterised by rupture into the left ventricle and intracranial haemorrhage as mentioned. The
presence and persistence of the hematoma required not only neurosurgical drainage but also a left temporal
craniotomy for evacuation. This atypical and exclusive presentation has not been reported in previous studies.
Conclusion. To conclude, the therapeutic management of neonatal brain abscess requires a multidisciplinary
approach involving paediatric neurosurgeons, anesthesiologists, and radiologists. Neurosurgical drainage
performed early by experienced hands seems to be the most effective approach in these high-risk paediatric
patients.